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BMC Pediatrics
|
July 30, 2011
Paediatric UK demyelinating disease longitudinal study (PUDDLS)
Michael Absoud, Carole Cummins, Wui K Chong, et al.
Molecular Genetics and Metabolism
|
March 16, 2010
Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: implications for molecular diagnosis
Danielle Crompton, Pauline K Rehal, Lesley MacPherson, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
January 19, 2024
Hemorheological, cardiorespiratory, and cerebrovascular effects of pentoxifylline following acclimatization to 3,800 m
Andrew R Steele, Connor A Howe, Travis D Gibbons, et al.
Physiological Reports
|
February 4, 2026
The effect of sex on the isolated and combined α- and β-adrenergic control of blood flow during handgrip in adults at high altitude: An exploratory study
Lauren E Maier, Emily R Vanden Berg, Lydia Simpson, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
April 21, 2012
Paediatric acquired demyelinating syndromes: incidence, clinical and magnetic resonance imaging features
Michael Absoud, Ming J Lim, Wui K Chong, et al.
Pediatric Radiology
|
August 1, 2018
Prospective multicentre evaluation and refinement of an analysis tool for magnetic resonance spectroscopy of childhood cerebellar tumours
Karen A Manias, Lisa M Harris, Nigel P Davies, et al.
The Journal of Physiology
|
December 15, 2025
Role of reactive oxygen species in mediating peripheral hypoxic vasodilation and sympathoexcitation at high altitude
Liam D Corr, Andrew J M Douglas, Elliott J Jenkins, et al.
Journal of Inherited Metabolic Disease
|
March 3, 2017
Expanding the phenotype in argininosuccinic aciduria: need for new therapies
Julien Baruteau, Elisabeth Jameson, Andrew A Morris, et al.
American Journal of Human Genetics
|
April 9, 2011
Loss-of-function mutations in RAB18 cause Warburg micro syndrome
Danai Bem, Shin-Ichiro Yoshimura, Ricardo Nunes-Bastos, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
BMC Pediatrics
|
July 30, 2011
Paediatric UK demyelinating disease longitudinal study (PUDDLS)
Michael Absoud, Carole Cummins, Wui K Chong, et al.
Molecular Genetics and Metabolism
|
March 16, 2010
Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: implications for molecular diagnosis
Danielle Crompton, Pauline K Rehal, Lesley MacPherson, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
January 19, 2024
Hemorheological, cardiorespiratory, and cerebrovascular effects of pentoxifylline following acclimatization to 3,800 m
Andrew R Steele, Connor A Howe, Travis D Gibbons, et al.
Physiological Reports
|
February 4, 2026
The effect of sex on the isolated and combined α- and β-adrenergic control of blood flow during handgrip in adults at high altitude: An exploratory study
Lauren E Maier, Emily R Vanden Berg, Lydia Simpson, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
April 21, 2012
Paediatric acquired demyelinating syndromes: incidence, clinical and magnetic resonance imaging features
Michael Absoud, Ming J Lim, Wui K Chong, et al.
Pediatric Radiology
|
August 1, 2018
Prospective multicentre evaluation and refinement of an analysis tool for magnetic resonance spectroscopy of childhood cerebellar tumours
Karen A Manias, Lisa M Harris, Nigel P Davies, et al.
The Journal of Physiology
|
December 15, 2025
Role of reactive oxygen species in mediating peripheral hypoxic vasodilation and sympathoexcitation at high altitude
Liam D Corr, Andrew J M Douglas, Elliott J Jenkins, et al.
Journal of Inherited Metabolic Disease
|
March 3, 2017
Expanding the phenotype in argininosuccinic aciduria: need for new therapies
Julien Baruteau, Elisabeth Jameson, Andrew A Morris, et al.
American Journal of Human Genetics
|
April 9, 2011
Loss-of-function mutations in RAB18 cause Warburg micro syndrome
Danai Bem, Shin-Ichiro Yoshimura, Ricardo Nunes-Bastos, et al.
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of 3